Canonical Allele Identifier: CA1024478600

Gene: BCR

Linked Data

• dbSNP Id: rs2073975387
• gnomAD v3: 22-23308749-G-GTCAA
• gnomAD v4: 22-23308749-G-GTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23308752_23308753insATCA , CM000684.2:g.23308752_23308753insATCA	GRCh38
NC_000022.10:g.23650939_23650940insATCA , CM000684.1:g.23650939_23650940insATCA	GRCh37
NC_000022.9:g.21980939_21980940insATCA	NCBI36
NG_009244.1:g.133388_133389insATCA
NG_009244.2:g.133388_133389insATCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305877.13:c.3013-672_3013-671insATCA MANE Select	ENSP00000303507.8:n.3013-672_3013-671insATCA
ENST00000305877.12:c.3013-672_3013-671insATCA	ENSP00000303507.8:n.3013-672_3013-671insATCA
ENST00000359540.7:c.2881-672_2881-671insATCA	ENSP00000352535.3:n.2881-672_2881-671insATCA
ENST00000398512.9:c.1709-672_1709-671insATCA	ENSP00000381524.6:n.1709-672_1709-671insATCA
ENST00000419722.6:n.238-672_238-671insATCA
ENST00000475025.5:n.87-672_87-671insATCA
ENST00000478978.5:n.294-672_294-671insATCA
NM_004327.3:c.3013-672_3013-671insATCA	NP_004318.3:n.3013-672_3013-671insATCA
NM_021574.2:c.2881-672_2881-671insATCA	NP_067585.2:n.2881-672_2881-671insATCA
NM_004327.4:c.3013-672_3013-671insATCA MANE Select	NP_004318.3:n.3013-672_3013-671insATCA
NM_021574.3:c.2881-672_2881-671insATCA	NP_067585.2:n.2881-672_2881-671insATCA